pink pigmented
METPO:1003027 · CLASS · REVIEWED
A pigmentation phenotype in which microbial colonies or cells appear pink due to accumulation of pink or rose carotenoid pigments.
Pink pigmentation carotenoid mechanism
Edge evidence
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isoprenoid precursors
feed into
carotenoid biosynthesis
Isoprenoid precursors provide substrate for carotenoid production.
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DOI:10.1016/j.gene.2004.11.038isoprenoid precursor biosynthesis
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Crt enzymes
catalyzes
carotenoid biosynthesis
biolink:catalyzesCrt enzymes catalyze reactions in carotenoid biosynthesis.
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DOI:10.1080/1040841X.2025.2526423crt genes ... reactions they catalyze
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carotenoid biosynthesis
has output
pink carotenoids
RO:0002234Carotenoid biosynthesis can produce pink bacterial pigments.
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DOI:10.1080/1040841X.2025.2526423pink ... pigmentation in bacteria
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pink carotenoids
causes
visible pink color
biolink:causesPink carotenoids cause visible pink pigmentation.
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DOI:10.1080/1040841X.2025.2526423responsible for the red, pink, orange, and yellow pigmentation
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visible pink color
manifests as
pink pigmented
METPO:2007400Visible pink color manifests the pink-pigmented phenotype.
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DOI:10.1080/1040841X.2025.2526423pink ... pigmentation in bacteria
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lycopene
precursor of
pink carotenoids
Lycopene is the central precursor converted into colored downstream carotenoid pigments.
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DOI:10.3390/biology12101346
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carotenoid biosynthesis
feeds from
lycopene
Carotenoid biosynthesis proceeds through lycopene toward colored carotenoid products.
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DOI:10.3390/biology12101346
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Crt enzymes
part of
photosynthesis gene cluster
biolink:part_ofcrt carotenoid genes are part of photosynthesis gene clusters in phototrophic bacteria.
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DOI:10.3390/biology12101346
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photosynthesis gene cluster
contributes to
visible pink color
RO:0002326Carotenoid genes embedded in photosynthesis gene clusters contribute to visible pigmentation.
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DOI:10.3390/biology12101346
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ambient molecular oxygen
upregulates
crtI-crtB operon
Oxygen availability upregulates the carotenoid biosynthetic operon, an environmental regulator of pigment output.
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DOI:10.3390/biology12101346
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crtI-crtB operon
catalyzes
carotenoid biosynthesis
biolink:catalyzesThe crtI-crtB operon encodes enzymes carrying out carotenoid biosynthetic reactions.
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DOI:10.3390/biology12101346
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1080/1040841X.2025.2526423
Parent traits (1)
Synonyms (1)
- Pigment_pink
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1003027[-4.184, -3.258, -1.095, +0.518, …]
Nearest neighbors in embedding space
- morphology pigmentation 0.839
- morphology white pigmented 0.820
- morphology carotenoid pigmentation 0.790
- morphology green pigmented 0.753
- morphology black pigmented 0.737
- morphology red pigmented 0.736
- morphology cream pigmented 0.699
- morphology orange pigmented 0.683
Deep research
# Curation report: microbial **pink pigmented** ## 1. Scope and recommended interpretation **Target:** `METPO:1003027` (quote verbatim) **Category:** morphology; **term kind:** class; **status:** reviewed **Parent:** `METPO:1003021` **Synonym:** *Pigment_pink* The trait should represent an **observed colony- or cell-level color phenotype**, not merely genomic capacity for carotenoid synthesis. Operationally, it is the appearance of a pink or rose color caused by intracellular or membrane-associated accumulation of colored metabolites, most often carotenoids. The strongest causal evidence retrieved is from *Methylobacterium extorquens* PA1: LC–MS and mutant/complementation experiments show that pigmentation depends on a **squalene-derived C30 carotenoid pathway**, rather than the previously presumed canonical C40 phytoene pathway (rizk2021functionaldiversityof pages 2-3). Pink is not chemically unique. In *Rhodotorula*, colony colors form an orange–salmon–pink–red continuum determined by pigment composition and concentration; reported carotenoids include β-carotene, γ-carotene, lycopene, torulene, and torularhodin. Thus, color alone does not identify a particular molecule or pathway (ochoavinals2024currentadvancesin pages 1-2). ### Boundary cases 1. **Pink versus red, salmon, or orange:** These are neighboring assay categories, not necessarily distinct pathways. Lighting, medium, colony age, pigment concentration, and observer thresholds can change the assigned color. 2. **Pigment-production capacity versus observed pigmentation:** A complete biosynthetic gene cluster predicts capacity but is insufficient for `METPO:1003027` unless pink color is actually observed. 3. **PPFM versus pink pigmentation:** “Pink-pigmented facultative methylotroph” combines color and C1 metabolism. Methanol growth is not part of this morphology trait and should be represented separately. 4. **Carotenoid pigmentation versus other pigments:** The supplied definition restricts the class to pink/rose carotenoids. Pink caused by unrelated pigments, medium indicators, adsorbed compounds, host material, or mixed cultures should not be included without revising the definition. 5. **Stress response versus constitutive morphology:** Stress-induced red-pink astaxanthin accumulation in *Phaffia rhodozyma* is relevant but conditional and taxon-specific, rather than a universal mechanism (florescotera2021decipheringthemechanism pages 1-2). ## 2. Current mechanistic understanding ### 2.1 Strongest bacterial mechanism: squalene-derived C30 carotenoids In *M. extorquens* PA1, all detected carotenoids had C30 backbones. Deleting `crtN` or `crtP` abolished pigmentation, and complementation restored it. By contrast, deleting `crtB`, associated with C40 phytoene production, did not alter pigmentation under the tested conditions. This establishes a causal chain from squalene production through the C30 pathway to visible pigmentation (rizk2021functionaldiversityof pages 2-3). The carotenoids occur in the outer membrane. Carotenoid-deficient mutants did not show major growth defects over 10–34°C or substantial membrane-permeability changes, but showed slightly increased hydrogen-peroxide/oxidative-stress sensitivity. Therefore, oxidative protection is a supported secondary function, but it should not be represented as necessary for pink color (rizk2021functionaldiversityof pages 9-11). ### 2.2 Fungal C40 carotenoid mechanisms Recent synthesis for *Rhodotorula* describes HMG-CoA-dependent isoprenoid precursor supply, `CRTYB`-encoded phytoene synthesis from geranylgeranyl diphosphate, and `CRTI`-mediated desaturation toward neurosporene and downstream carotenoids. γ-Carotene precedes β-carotene and torulene, while torulene is hydroxylated and oxidized to torularhodin. These reactions explain pink-to-red yeast pigmentation, but they must not be merged with the bacterial C30 mechanism as though they were one universal pathway (ochoavinals2024currentadvancesin pages 2-5). For *Rhodotorula* sp. CP72-2, genome analysis found putative `CrtE`, `CrtYB`, `CrtI`, `CrtS`, `CrtR`, `CrtW`, `CrtO`, and `CrtZ` genes. Because these assignments were genomic candidates rather than individual knockout or enzyme-kinetic demonstrations, they are lower-confidence causal nodes (kingkaew2023genomicinsightand pages 1-2). ### 2.3 Environmental control In *P. rhodozyma*, nitrogen or copper limitation, antimycin A, and mutations affecting respiration or nitrogen metabolism are associated with intense red-pink astaxanthin accumulation. The proposed convergence mechanism is an NADH/NAD+ imbalance in an oxidative environment, but the source explicitly treats the complete signaling mechanism as unresolved (florescotera2021decipheringthemechanism pages 1-2). In *Rhodotorula*, light, pH, salts, metals, and carbon-to-nitrogen ratio influence carotenoid accumulation. Low C/N generally favors carotenoids, whereas high C/N promotes lipids. These are fermentation- and strain-dependent modifiers rather than defining causes of the trait (ochoavinals2024currentadvancesin pages 1-2, ochoavinals2024currentadvancesin pages 2-5). ## 3. Candidate nodes ### Trait and observational nodes - `METPO:1003027` — pink pigmented - `METPO:1003021` — supplied parent trait - pink/rose colony pigmentation — label-only observational node - orange, salmon, red pigmentation — label-only boundary states - pigment concentration — experimental/quantitative factor - colony age, growth medium, illumination, observation method — assay factors ### Pathways and biological processes - C30 carotenoid biosynthesis from squalene — label-only pathway; strongest in *M. extorquens* PA1 - C40 carotenoid biosynthesis from geranylgeranyl diphosphate — label-only pathway - carotenoid biosynthetic process — `GO:0016117` - isoprenoid biosynthetic process — use only after identifier verification in the target ontology release - oxidative-stress response — label or verified GO term during implementation - carotenoid accumulation — label-only process
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_WITH_LITERATURE · codex
Added DOI-backed definition and causal graph for isoprenoid precursors, Crt enzymes, carotenoid biosynthesis, pink carotenoids, and visible pink color.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:catalyzes×1, biolink:causes×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007400×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0016117×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 6 evidence-backed generic edges (4 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:part_of×1, RO:0002326×1, biolink:catalyzes×1).
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:15948×1, ENVO:01001495×1).
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MIGRATE_MICROBE_DOMAIN_EDGES · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates (1 to has output), issue 301. The previous predicates are transitively rdfs:subPropertyOf METPO:2000001, whose rdfs:domain is METPO:1000525 (microbe), so a causal-graph subject entailed that the subject IS a microbe; CausalNodeTypeEnum has no organism member, so no such edge could ever satisfy the domain. Edge directions are unchanged - this pass only relabels and re-grounds. RO:0002234 (has output) is used where the subject is an activity, since biolink gives it the domain 'biological process or activity'; the METPO replacements are proposed in proposals/metpo_traitmech_v8 and v9 and are placeholder ids until METPO mints them.
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NORMALISE_NODE_TYPE · claude
Under the PATHWAY-vs-BIOLOGICAL_PROCESS rule, one node_id means one thing corpus-wide (issue 356): carotenoid_biosynthesis is typed PATHWAY. PATHWAY is a named, conventionally enumerable multi-step route; BIOLOGICAL_PROCESS is everything else. A named biosynthetic route. Most descriptions call it one outright, including BIOLOGICAL_PROCESS-typed ones ('Enzymatic pathway producing carotenoid pigments'); red_pigmented.yaml instead ENUMERATES the steps -- 'Phytoene synthase condenses two GGPP to phytoene, then desaturation/isomerization yields lycopene' -- which is the rule's own test for PATHWAY met explicitly rather than by naming. Applied AGAINST the majority, which was 5 BIOLOGICAL_PROCESS to 1 before this tranche.
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NORMALISE_NODE_SENSE · claude
One node_id per SENSE (issues 356, 384): ambient_oxygen is the chemical sense here. Already the ambient sense. Listed so a re-run still normalises the label and still retracts ENVO:01001495 if it has been re-applied — the grounder keys on (label, node_type), so an un-normalised label is what lets the retracted CURIE come back.